Validation Specialist Jobs

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CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Validation Specialist West Caldwell, NJ Full-Time Unspecified Apply Apply Validation Specialist West Caldwell, NJ Full-Time Unspecified Apply Job Details If you are a Validation Specialist with experience, please read on! What You Will Be Doing - Applying FDA, and other applicable global regulations ...

Regular Country United States State/Province Massachusetts City Boston Area of Expertise Engineering Company Summary Founded in 1911, SNC-Lavalin is one of the leading engineering and construction groups in the world and a major player in the ownership of infrastructure. From its offices in over 40 countries, SNC-Lavalin provides EPC and EPCM services to clients in a variety of industry ...

Job Description : Parexel is currenlty hiring a Sr. Validation Specialist to provide technical expertise, resource and support for the implementation, computerized system validation (CSV) and ongoing maintenance activities related to systems used by PAREXEL in the provision of their services. Work to the appropriate corporate standards of quality and efficiency, SOPs/Guidelines, ICH-GCP and/or ot...

THE CLEAREST PATH TO CAREER FULFILLMENT STARTS WITH PAREXEL. At PAREXEL, we believe that the power to work independently and intelligently should be yours every day. Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. On your PAREXEL journey, we support you with leading-edge...

CyberCoders Matching Great People with Great Companies Learn more about CyberCoders QA Validation Specialist - SQL West Caldwell, NJ Contract Unspecified Apply Apply QA Validation Specialist - SQL West Caldwell, NJ Contract Unspecified Apply Job Details If you are a QA Validation Specialist with SQL experience, please read on! What You Will Be Doing - Applying FDA, and other applica...

Quality Control_ Specialist II, Lab Validation Business Unit: Technical Ops SZ Division: SANDOZ Company/Legal Entity: Sandoz Job Reference Code: 165427BR PURPOSE Ensure compliance with respect to all QC and ARD instruments and software. Provides daily, on-the-floor support to the analysts and instruments. Uses project management and process improvement skills to optimize business activities....

Computer System Validation Specialist Job Summary In need of several Computer Systems Validation Specialists for a contract assignment at a pharmaceutical company in the Atlanta, Georgia area. The contract is expected to go until October 2015. One must be willing to travel up to 100% and preferably located in the southeast of the US. Great opportunity for someone with 3-5 years of computer system...

Job ID 161378BR Posting Title Sr. Validation Specialist Division PHARMA Business Unit CELL & GENE THERAPIES UNIT Country USA Work Location Morris Plains Company/Legal Entity Novartis Pharmaceuticals Functional Area Technical Operations Job Type Full Time Employment Type Regular Job Description Prepares/update validation master plan, project plans, and protocols; execute test plans, colle...

Job ID 165427BR Posting Title Quality Control_ Specialist II, Lab Validation (Lab Equipment Focus) Division SANDOZ Business Unit Technical Ops SZ Country USA Work Location Broomfield, CO Company/Legal Entity Sandoz Inc Functional Area Quality Job Type Full Time Employment Type Regular Job Description PURPOSE Ensure compliance with respect to all QC and ARD instruments and software. Prov...

ICF International is currently hiring a Certification & Accreditation Support Specialist / Policy Validator to work with an innovative team at Army Research Labs (ARL) in Adelphi, MD - College Park, MD. Together with ARL our Cybersecurity teams bring together government, industry and academia to advance the field of Cybersecurity through Cyber Research. As a member on the Agent of the Certificat...

Primary Duties and Responsibilities: · Responsible for planning, scheduling, execution and leading validation project assignments in coordination with the IT Manager and in accordance with Good Laboratory Practices (GLPs) and FDA 21 CFR Part 11. · Validation assignments include validation, qualification, and implementation of new and existing, processes, equipment, software, and instrumentation ...

Conducts the cleaning validation/verification studies including protocol preparation, strategy and the coordination of the studies with operations to insure equipment availability Coordinates the testing of samples with site chemistry and site microbiology Assessment of solubilities and toxicities for determining cleaning requirements Assist with the revision of site Cleaning Validation SOPs an...

Seeking Validation Engineers for a consulting position at a pharmaceutical client in Fort Worth, TX 76134. This contractor is needed to support periodic revalidations and ongoing equipment and process validations in order to maintain regulatory compliance. Education/Experience: Bachelors Degree in chemistry, engineering, or similar and 1-5 years applicable experience. Note: Experience could be ...

The Model Validation Specialist, VP is responsible for guiding independent reviews and validation of various models used by the Bank by assessing the underlying model assumptions, theoretical basis, and data used by models, as well as the processing, accuracy of output, and reporting. The Model Validation Specialist, VPis responsible for maintaining an inventory and definition of models, which inc...

QA Equipment Validation Specialists are part of the Quality organization and report directly to the QA Validation Manager. Lead all validation activities for commissioning of a cell therapy facility in both supervised and unsupervised areas. Work closely with a dedicated project team to manage activities to the required deadlines. Facilitate discussions and provide strategic guidance on commissi...

BRIEF SUMMARY: This is an entry level position, requiring a minimum of 1 year of experience in specific C2 Elements, Subsystems, Systems and Capabilities, preferably CEC. Provides systems engineering expertise relevant to Track Management (TM) test and evaluation support, requirement identification and tracking, documentation, and working group support. Scope includes services provided for Navy ...

ARGOS IS GROWING! Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases based on its Arcelis™ technology platform. We are currently seeking a well-qualified QA Validation Specialist. SCOPE: Provide QA oversight of Validation programs at Argos, including review an...

Associated Validation Specialist/Engineer Mangan Biopharm is seeking applications for the position of Associate Validation Specialist or Engineer in the Raleigh-Durham area. This person will be responsible for developing documentation for automation projects in the biotech and pharmaceutical industries. This person will perform the following tasks: · Updates of Design Specifications · Technical...

VALIDATION SPECIALIST: work in King of Prussia. Lead efforts by coordinate activities of Validation, Quality & other groups required to manage projects through the CAPA, CC, Annex 11, 21 CFR Part 11 & GAMP5. Prepare/ update validation documents such as Assessments, VPP, SLIA, CCA, URS, FRS, DS, SOP's IQ, OQ and PQ protocols, VSR, RTM, VMPA and VMRA. Min: MS in Chemistry w/ 12 mo related exp. Send ...

Currently we have a temporary opening for a Validation Specialist to support a company located in the Swiftwater, PA area.   Responsibilities: Responsible for reviewing data that is generated from the adverse event system to verify that it is accurate and consistent with the request from the safety officer. Responsible for working with the subject matter experts (SME) and the ad hoc program sp...